Top 57 quality specialist Jobs in durham nc

Complaint Reporting MDR/Vigilance Specialist 2
Teleflex —Morrisville, NC
- Nursing
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Quality Control Specialist
Greenology Products, LLC —Raleigh, NC
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health savings account
- Health insurance
Quick Apply
2d
Electrical Quality Specialist
Adams Electric Company —Raleigh, NC
- $22 - $35 an hour
- On call
- Construction site
- Mid-level
- Analysis skills
Quick Apply
Clinical Quality Specialist
SonderMind —Durham, NC
- $72,000 - $82,000 a year
- Full-time
- Remote
- LMFT
- Licensed Clinical Social Worker
- Mid-level
- Commuter assistance
- Paid parental leave
Quick Apply
KBI: US - QA Specialist II
KBI Biopharma —Durham, NC
- $55,000 - $86,900 a year
- Full-time
- Laboratory experience
- Mid-level
- High school diploma or GED
Senior QA Specialist, External Manufacturing, US
Bavarian Nordic —Durham, NC
- $120,000 - $155,000 a year
- Full-time
- Remote
- Travel
- Senior level
- Communication skills
13d
Early Career Construction Materials Testing Professional
WSP —Durham, NC
- Background check
- Construction site
- Pass drug screening
Sr. Quality Assurance Specialist
Asklepios BioPharmaceutical —Durham, NC
- Full-time
- 5 years
- Laboratory experience
- Office
Clinical Quality Assurance Specialist - Trauma Program
UNC Health —Chapel Hill, NC
- $35.87 - $51.57 an hour
- Full-time
- Hybrid work
- Nursing
- RN License
- Research
KBI: US - Principal QA Specialist
KBI Biopharma —Durham, NC
- $113,000 - $156,000 a year
- Full-time
- 6 years
- Master's degree
- Bachelor's degree
QA Specialist II
KBI Biopharma —Durham, NC
- Full-time
- Word processing
- Bachelor of Science
- 8 years
Quality Risk Specialist
Grifols —Durham, NC
- Full-time
- Hybrid work
- Master's degree
- Ability to lift 50 pounds
- Analysis skills
QA Manufacturing Specialist II
KBI Biopharma —Durham, NC
- Full-time
- Bachelor of Science
- Mid-level
- 3 years
12d
QC Regulatory & Stability Area Specialist
Novo Nordisk —Durham, NC
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
- Paid holidays
- Disability insurance
7d
Quality Assurance Specialist - Quality Systems - 3 OPENINGS
Amgen —Holly Springs, NC
- $104,287.35 - $141,094.65 a year
- Doctoral degree
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
5d
Quality & Compliance Specialist
Axil Health —Raleigh, NC
- Mid-level
- Analysis skills
- Bachelor's degree
Quick Apply
Sr/Principal Computer Systems Validation Specialist
KBI Biopharma —Durham, NC
- $118,000 - $183,700 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Quality Specialist - cGMP Manufacturing - Weekend 1st Shift
Alcami Corporation —Morrisville, NC
- Full-time
- Ability to walk for extended periods
- Basic math
- Data analysis skills
Clinical Quality Assurance Specialist - Bone Marrow Transplant Program
UNC Health —Chapel Hill, NC
- $35.87 - $51.57 an hour
- Full-time
- Hybrid work
- Nursing
- RN License
- Mid-level
5d
Professional Test Driver
VinFast US —Raleigh, NC
- Seasonal
- Mid-level

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Complaint Reporting MDR/Vigilance Specialist 2

Teleflex -
Morrisville, NC

Quick Apply

Job Details

Qualifications

Customer communication
Microsoft Excel
Microsoft Outlook
Bachelor's degree
Biomedical regulatory compliance
Quality systems
ISO 13485

Full Job Description

Date: May 29, 2026

Location: Morrisville, NC, US

Company: Teleflex

Expected Travel: Up to 10%

Requisition ID: 13762

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

Position Summary

Work within Complaint Intake & Reporting team to critically review complaints to determine reportability based on the regulatory requirements, risk documentation and clinical experience. Responsible for preparation and timely submissions of MDR/Vigilance reports to FDA/Competent Authorities and other regulatory agencies. Where necessary, seek and document relevant additional information in line with the complaint intake process. Identify potential issues to continuously improve process.

Principal Responsibilities

Utilizes clinical experience in conjunction with risk management documentation to review complaints for adverse event reportability in accordance with US Canadian & European regulations within required time frames.
Follows up with health care providers and customers to provide clarification for complaint files and document correspondence to complaint files as required.
Prepare and submit regulatory reporting documentation such as MedWatch forms with FDA and Vigilance Reports with Canadian and European regulatory authorities.
Assist as clinical liaison for the complaint management department to facilitate understanding of clinical application for product complaint devices and provide training to other team members as required.
Utilize complaint management system to accurately document complaint information.
Final Reviewer/Approval of reporting decisions and initial reports
Support audit activities are required. Assists with responses to FDA and Competent Authority for additional information queries.
Work to meet team KPI’s Department Metrics and over QA/RA goals and objectives.
Support improvement projects in the complaint intake and reporting function.
Support wider QMS and risk management activity as required.

Education / Experience Requirements

B.S. Degree in Nursing, Biomedical Engineering, or related science discipline

1-3 years medical device experience
Experience in Post-Market Surveillance with a preference for experience in Complaint Handling/Vigilance Reporting.
Demonstrated knowledge of Medical Device Quality Systems regulations, including FDA’s 21 CFR 820, 21 CFR 803, ISO 13485:2016, MDD, EU MDR, MDSAP.

Specialized Skills / Other Requirements

Ability to critically review information and seek clarification.
Ability to work well under deadlines and pressure in a changing environment.
Skilled in use of Microsoft suite of applications i.e., Excel, Outlook, and Word.
The ability to prioritize tasks and manage several tasks simultaneously.
Ability to read understand and self-educate on emerging regulatory requirements.

BEHAVIORS / VALUES

Self-driven and ability to work independently and/or as a team player.
Approachable and enthusiastic. Flexible and adaptable.
Good judgment and problem-solving ability & is capable of understanding the impact of decision making on both Teleflex Medical and their customers.
Experience with risk management - preferred.
Experience with a high-volume complaints environment - preferred.
Strong organizational, time management, and influence skills with cultural awareness and sensitivity
Excellent verbal and written communication skills with ability to lead meetings.

#LI-AD1

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or [email protected].

Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

Nearest Major Market: Raleigh

Application Question(s):

Do you require sponsorship, now or in the future, to work in the US?

Ability to Commute:

Morrisville, NC 27560 (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

quality specialist jobs in durham nc

Complaint Reporting MDR/Vigilance Specialist 2

Quality Control Specialist

Electrical Quality Specialist

Clinical Quality Specialist

KBI: US - QA Specialist II

Senior QA Specialist, External Manufacturing, US

Early Career Construction Materials Testing Professional

Sr. Quality Assurance Specialist

Clinical Quality Assurance Specialist - Trauma Program

KBI: US - Principal QA Specialist

QA Specialist II

Quality Risk Specialist

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Quality Assurance Specialist - Quality Systems - 3 OPENINGS

Quality & Compliance Specialist

Sr/Principal Computer Systems Validation Specialist

Quality Specialist - cGMP Manufacturing - Weekend 1st Shift

Clinical Quality Assurance Specialist - Bone Marrow Transplant Program

Professional Test Driver

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